Benzamides

2,6-Dimethoxyaniline is a synthetic compound that has been used in the past as an antibacterial agent. It has been shown to be effective against Staphylococcus aureus and Escherichia coli, but not against Pseudomonas aeruginosa. 2,6-Dimethoxyaniline forms nanowires with an average diameter of 100 nm and lengths up to 1 micron when exposed to radiation (e.g., gamma rays). The reaction rate is dependent on the architecture and morphology of the azobenzene moiety. The chloride anion coordinates with the nitrogen atom in the molecule, which leads to a phase transition temperature of about 230 K.

3-Chloro-4-fluoroaniline is a versatile building block that can be used in the synthesis of many different compounds. It is a reagent that is used in research, where it can be used as a reactant or an intermediate. This chemical has been shown to have high quality and can be used as a starting material for the synthesis of other chemicals. 3-Chloro-4-fluoroaniline has been shown to react with various functional groups such as amines and acid chlorides. It is also useful for the construction of scaffolds, which are three dimensional structures that are built from small molecules and organic compounds. 3-Chloro-4-fluoroaniline is classified as a speciality chemical and its CAS number is 367-21-5.

3,5-Dibromoaniline is a chemical compound that belongs to the group of anilines. It can be used as an intermediate in organic synthesis. 3,5-Dibromoaniline can be obtained by gravimetric analysis and has a solute of about 0.1 g/100 mL in water. The melting point for this compound is about 245 °C and the boiling point is about 330 °C at normal atmospheric pressure. 3,5-Dibromoaniline has been shown to inhibit the growth of Trichophyton mentagrophytes and Coumarin derivatives, which are fungi that cause ringworm infections. This drug also has photophysical properties and can be used as a fluorescence probe for DNA hybridization studies.

Please enquire for more information about cis-2-(3,4-Difluorophenyl)cyclopropan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Fluoro-6-hydroxybenzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,4,6-Trimethoxyaniline is an organic compound with a variety of uses. It is a precursor for many pharmaceuticals and can be used as an intermediate in the synthesis of other compounds. 2,4,6-Trimethoxyaniline has been shown to inhibit bacterial growth by inhibiting the synthesis of DNA and protein. This compound has also been shown to have antibacterial activity against gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes. It also inhibits the production of inflammatory mediators such as prostaglandin E2 (PGE2) that are involved in inflammation.

2,6-Diiodo-4-nitroaniline is a complex molecule that consists of a ferrocene and an amide. It is insoluble in water and has a low solubility in organic solvents. The molecule was synthesized by reacting 2,6-dichloroaniline with ferric chloride. The molecule has been shown to have high efficiencies when used as a catalyst for the oxidation of chlorobenzene. This compound also reacts with phenols to form quaternary ammonium salts, which are useful for the extraction of metal ions from water. 2,6-Diiodo-4-nitroaniline can be conjugated with diacids or amides to form new compounds that are soluble in organic solvents.

Please enquire for more information about 3,5-Difluoro-4-(methylsulfanyl)aniline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Methoxy-4-(methylsulfanyl)aniline hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,6-Dinitro-4-methylaniline is an amide that has been shown to induce cancer in animals. It has a high affinity for nucleic acids and forms covalent bonds with DNA. 2,6-Dinitro-4-methylaniline is metabolized by the liver and excreted by the kidneys into urine, where it can be detected in urine samples. This compound has been shown to bioconcentrate in organisms and accumulate in tissues as well as activate radiation. The activation of this compound is dose dependent and may be due to its ability to form covalent bonds with DNA.

Fmoc-beta-alanine is a type of amino acid that is found in plants. It has been shown to have biological properties and can be used as an ingredient in food products. Fmoc-beta-alanine is also a chemical ligation agent that can be used for the synthesis of cyclic peptides and polypeptides. The compound has been shown to inhibit chloride ion channels, which may make it useful for the treatment of autoimmune diseases. Fmoc-beta-alanine is natural antibacterial and has been shown to increase the activity of urokinase-type plasminogen activator, which may make it useful for the treatment of cardiovascular diseases. Fmoc-beta-alanine is a sequence of amino acids found in wheat germ, as well as other plant families such as corn and rice. This compound binds to specific receptors and can be synthesized by solid phase synthesis on a resin column.

2-Chloro-3-methoxyaniline is a high quality chemical. It is an intermediate in the synthesis of other complex compounds and has been used as a reagent for organic synthesis. It is also useful as a building block for the preparation of speciality chemicals, research chemicals, and versatile building blocks. 2-Chloro-3-methoxyaniline reacts with other chemicals to form new compounds that are useful for pharmaceuticals and agrochemicals.

2,2'-Dithiodianiline is a redox-active molecule with a redox potential of -0.08 V. It has been shown to inhibit the polymerase chain reaction by binding to DNA and inhibiting the enzyme DNA polymerase. 2,2'-Dithiodianiline is a potent inhibitor of bacterial growth in vitro, and has been shown to be cytotoxic in vivo. 2,2'-Dithiodianiline inhibits the growth of resistant mutants that are resistant to other antibiotics such as penicillin and ampicillin. This compound binds to molybdenum at an optimum concentration of 0.5 mM and coordinates through electrostatic interactions with the molybdenum atom. Structural analysis reveals that 2,2'-dithiodianiline forms hydrogen bonds with adenine residues in DNA and interacts with guanine residues in RNA through π-π stacking interactions. This interaction prevents transcription by blocking the binding

2,4,6-Trimethoxyaniline is a tetrazole compound that has been shown to inhibit glycosidases. The inhibition of these enzymes prevents the hydrolysis of glycosidic bonds in carbohydrates and other biomolecules. 2,4,6-Trimethoxyaniline is used as an antibacterial agent against methicillin-resistant Staphylococcus aureus (MRSA) and other bacteria. It also inhibits the growth of Mycobacterium tuberculosis and Mycobacterium avium complex due to its ability to inhibit protein synthesis by inhibiting RNA synthesis. 2,4,6-Trimethoxyaniline can be synthesized by demethylation of anisidine with tribromide or chloroform.

2-Mercapto-N-methylbenzamide is a synthetic compound that has been shown to have inhibitory activities against activated brain cells and cell lines. This drug has been used in the synthesis of axitinib, a cancer drug that inhibits cellular growth. 2-Mercapto-N-methylbenzamide is also used as a preservative in cosmetics and can be found in carbonated drinks and foods. It has been shown to inhibit the production of serotonin in microbicidal reactions by inhibiting the enzyme hydroxymethyl transferase, which catalyzes the conversion of 5-hydroxytryptophan to serotonin. It also prevents the reaction products from being formed by reacting with hypoxanthine, xanthine, and phosphoribosyl pyrophosphate (PRPP). 2-Mercapto-N-methylbenzamide also reacts with plasma samples to form ethylmercaptoacetate, which is then oxidized to merc

2-Hydroxy-4-methoxybenzamide is a pesticide that belongs to the group of amides. The compound inhibits the biosynthesis of tyrosine by binding to the enzyme tyrosinase and interrupting its activity. 2-Hydroxy-4-methoxybenzamide also has an interaction with other pesticides, such as remoxipride, which may be due to intramolecular hydrogen bonding. This interaction may lead to an increase in the toxicity of these pesticides. Molecular modeling studies have shown that 2-hydroxy-4-methoxybenzamide forms hydrogen bonds with the salicylaldehyde molecule.

Please enquire for more information about 2-(4-Aminobenzyl)aniline including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Methoxybenzamide is a small molecule that has been shown to have anticancer activity in vitro and in vivo. It is a hydroxylated benzamide with an intramolecular hydrogen bond, which allows it to selectively bind to DNA at the C4' position of cytosine. The compound's anticancer effects are due to its ability to inhibit the transcription of genes involved in cancer cell proliferation and its ability to induce apoptosis via caspase activation. 4-Methoxybenzamide has been shown to be synergistic when used with other chemotherapeutics, such as cisplatin, doxorubicin or 5-fluorouracil. This drug also inhibits the uptake of these drugs by cancer cells, limiting their therapeutic effects on healthy tissues.

Dansylamidoethyl mercaptan is a molecule that reacts with the -SH group of proteins and other thiol-containing molecules. It has been shown to react with biological samples in vitro, and also has been shown to have biological properties. Dansylamidoethyl mercaptan binds to protein cysteine residues through covalent adduct formation and may be used as a probe for S-S bonds in proteins. This molecule can form reactive electrophiles that may cause allergic reactions on skin contact. It has been shown to react with usnic acid, nonetheless, it does not react with ascaridole or thp-1 cells.